Status:

UNKNOWN

GDF 15 in Sickle Cell Disease and Hereditary Spherocytosis

Lead Sponsor:

Wolfson Medical Center

Conditions:

Patients With Thalassemia Intermedia,

Congenital Dyserythropoietic Anemia Type I

Eligibility:

All Genders

5+ years

Brief Summary

Patients with thalassemia intermedia, congenital dyserythropoietic anemia type I , and sideroblastic anemia were found to express very high levels of serum GDF15, and this contributed to the inappropr...

Detailed Description

The identification of the ferroportin/hepcidin axis has allowed the effect of erythroid activity on iron balance to be studied and has created the basis for better defining the erythroid regulators. ...

Eligibility Criteria

Inclusion

  • non

Exclusion

  • non

Key Trial Info

Start Date :

September 1 2010

Trial Type :

OBSERVATIONAL

Allocation :

ESTIMATED

End Date :

September 1 2011

Estimated Enrollment :

80 Patients enrolled

Trial Details

Trial ID

NCT01201135

Start Date

September 1 2010

End Date

September 1 2011

Last Update

September 14 2010

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